CLINICAL TRIALS
This is what ADAX can ensure for interventional trials:
- Study feasibility and site selection
- Collection and review of essential documents
- Submissions to the Ethics Committees and Regulatory Authorities
- Preparation, negotiation and execution of contracts with sites
- Site Initiation, including training related to specific clinical trial
- Good Clinical Practice (GCP) training for physicians and other research staff
- Organization and execution of investigator meetings
- Monitoring of clinical trials
- Project management of your clinical trial
- Study Close-Out activities
- Translations of study documents
- Preparation of study files
- Study materials management
- Data Management and Biostatistics
- Preparation and set-up of (e)CRF